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Details

Stereochemistry RACEMIC
Molecular Formula C15H18N3O4.H4N
Molecular Weight 322.3596
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Imazamox-Ammonium

SMILES

[NH4+].COCC1=CN=C(C2=NC(C)(C(C)C)C(=O)N2)C(=C1)C([O-])=O

InChI

InChIKey=GNZZHGJSMCDMBU-UHFFFAOYSA-N
InChI=1S/C15H19N3O4.H3N/c1-8(2)15(3)14(21)17-12(18-15)11-10(13(19)20)5-9(6-16-11)7-22-4;/h5-6,8H,7H2,1-4H3,(H,19,20)(H,17,18,21);1H3

HIDE SMILES / InChI

Molecular Formula C15H19N3O4
Molecular Weight 305.3291
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula H3N
Molecular Weight 17.0305
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Haptens and monoclonal antibodies for immunoassay of imidazolinone herbicides.
2002 Jun 5
Cross resistance to ALS-inhibiting herbicides in Euphorbia heterophylla L. biotypes resistant to imazethapyr.
2003
Evaluation of resistance in Amaranthus quitensis Kunth populations to imazethapyr and other imidazolinones.
2003
Biomassbed: a biological system to reduce pesticide point contamination at farm level.
2004 May
Quantitative analysis of imazamox herbicide in environmental water samples by capillary electrophoresis electrospray ionization mass spectrometry.
2004 May 21
A comparative risk assessment of genetically engineered, mutagenic, and conventional wheat production systems.
2005 Dec
Does the effect of herbicide pulse exposure on aquatic plants depend on Kow or mode of action?
2005 Feb 10
Photochemical degradation of imazamox in aqueous solution: influence of metal ions and anionic species on the ultraviolet photolysis.
2006 May 17
Cross-resistance profile of mesosulfuron-methyl-resistant Italian ryegrass in the southern United States.
2007 Apr
Molecular and biochemical characterization of an induced mutation conferring imidazolinone resistance in sunflower.
2008 Dec
Comparative genotoxicity evaluation of imidazolinone herbicides in somatic cells of Drosophila melanogaster.
2008 Jan
Isolation, characterization of a strain capable of degrading imazethapyr and its use in degradation of the herbicide in soil.
2009 Oct
[Isolation, identification and soil remediation of atrazine-degrading strain T3 AB1].
2010 Dec
Identification of a hybridization window that facilitates sizeable reductions of pollen-mediated gene flow in spring wheat.
2010 Jun
Activity profiles of 309 ToxCastâ„¢ chemicals evaluated across 292 biochemical targets.
2011 Mar 28
Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays.
2013 Jun 17
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 11:10:05 GMT 2023
Edited
by admin
on Sat Dec 16 11:10:05 GMT 2023
Record UNII
TUI70EI1Y7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Imazamox-Ammonium
ISO  
Common Name English
IMAZAMOX-AMMONIUM [ISO]
Common Name English
BEYOND
Brand Name English
IMAZAMOX AMMONIUM SALT
Common Name English
3-PYRIDINECARBOXYLIC ACID, 2-(4,5-DIHYDRO-4-METHYL-4-(1-METHYLETHYL)-5-OXO-1H-IMIDAZOL-2-YL)-5-(METHOXYMETHYL)-, MONOAMMONIUM SALT
Systematic Name English
Code System Code Type Description
FDA UNII
TUI70EI1Y7
Created by admin on Sat Dec 16 11:10:05 GMT 2023 , Edited by admin on Sat Dec 16 11:10:05 GMT 2023
PRIMARY
PUBCHEM
18772481
Created by admin on Sat Dec 16 11:10:05 GMT 2023 , Edited by admin on Sat Dec 16 11:10:05 GMT 2023
PRIMARY
EPA CompTox
DTXSID00904418
Created by admin on Sat Dec 16 11:10:05 GMT 2023 , Edited by admin on Sat Dec 16 11:10:05 GMT 2023
PRIMARY
CHEBI
133232
Created by admin on Sat Dec 16 11:10:05 GMT 2023 , Edited by admin on Sat Dec 16 11:10:05 GMT 2023
PRIMARY
CAS
247057-22-3
Created by admin on Sat Dec 16 11:10:05 GMT 2023 , Edited by admin on Sat Dec 16 11:10:05 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE